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<h3>Job Description</h3>
Job Description
Tolunay-Wong Engineers, Inc. is seeking a Geotechnical Engineer for our Houston Area offices.&nbsp; The successful candidate will provide engineering and consulting services for a wide variety of projects and clients in variety of market sector. &nbsp;We will provide training and support necessary for career advancement with the objective of developing the candidate into a departmental management role.&nbsp; Our Houston operations are well established in the local market and our offices have an experienced engineering support staff in place. We are seeking a candidate with excellent communication skills, a strong desire for career advancement, and sound leadership qualities. RESPONSIBILITIES
<ul>
<li>Prepare technical proposals.</li>
<li>Execute geotechnical engineering project assignments.</li>
<li>Work with and provide mentorship of engineering support staff.</li>
<li>Manage and coordinate geotechnical field and laboratory assignments.</li>
<li>Perform engineering analyses and report preparation.</li>
</ul>
<ul>
<li>Maintain client expectations for project quality and schedule. </li>
</ul>
REQUIREMENTS
<ul>
<li>Bachelor&nbsp;Degree in Civil Engineering</li>
<li>PE License or Active EIT Certification</li>
<li>Excellent written and verbal communication skills.</li>
</ul>
BENEFITS TWE provides its full-time employees with a benefit package that is inclusive of the following:
<ul>
<li>Flexible work schedule</li>
<li>Health Insurance, Vision,&nbsp;Dental,&nbsp;Disability and Life Insurances.</li>
<li>401(k) Retirement Program with up to 4% employer match after eligibility period.</li>
<li>120 hours of Paid Time Off (PTO) annually</li>
<li>9 company paid holidays</li>
</ul>
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OYK36lMeng

Geotechnical Engineer (Civil Eng. Degree Only)

<h3>Job Description</h3>
Job Description
We have an immediate opportunity for a Wildlife Biologist in the Southern and Northern California area. The ideal candidate will be responsible for managing individual project tasks and providing direction to the support staff.
Duties and Responsibilities
<ul>
<li>Ability to multitask with strong organization skills supporting the team and project management</li>
<li>Experience preparing and reviewing application and regulatory documents</li>
<li>Ability to prepare project scopes and proposals</li>
<li>Knowledge preparing and managing project schedules</li>
<li>Attend project and agency meetings</li>
<li>Manage field surveys as needed</li>
<li>Mentor entry-level and junior field staff</li>
</ul>
Background and Education
<ul>
<li>Bachelor’s Degree in natural science, field, Master’s or PhD a plus</li>
<li>3 years’ related work experience including project and task management</li>
<li>Previous experience working with regulatory processes. Must understand the federal Clean Water Act Section 404 and 401; Porter Cologne Water Quality Act; CDFW Fish and Game Code 1602; California ESA 2081; and ESA Section 7 and 10 processes.</li>
<li>Experience with wetland delineations and/or other local flora and fauna field surveys</li>
<li>Knowledge of California biological habitats, species and general conservation biology/ecology</li>
<li>USFWS/CDFW permits and Memoranda of Understanding a plus</li>
<li>Excellent communication and writing skills.</li>
</ul>
We offer a generous benefits package including company-paid medical insurance, paid holidays, 401k and paid time off (PTO)
Upon a conditional job offer, a drug test and background check will be required.
Compensation based on experience.
(Biologist, Master’s, PhD, CDFW, USFWS, Species, Flora, Fauna, habitat, 404)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

Wildlife Biologist

<h3>Job Description</h3>
Job Description
We have immediate opportunity for all levels of Wildlife Biological Monitors for the Central Valley Area. MUST have Wildlife Biological Monitoring Experience in California.
VARIOUS DUTIES AND RESPONSIBILITIES (other duties may be assigned)
<ul>
<li>Experience and knowledge of wildlife species in the Central Valley including small mammals, birds, and reptiles.</li>
<li>Familiarity with state and federal regulations, knowledge of environmental regulatory process is a must.</li>
<li>Experience with monitoring all ground distributing activity including mass grading, grubbing, weed abatement, trenching and any excavation on previously disturbed and undisturbed ground.</li>
<li>Does or oversees field inspections of proposed project areas.</li>
<li>Perform biological monitoring at construction sites to implement mitigation measures.</li>
<li>Conduct field surveys.</li>
<li>Record data for scientific and compliance purposes using company forms and established field methodology.</li>
<li>Ability to read maps.</li>
<li>Prepare daily progress/monitoring reports as needed by the project.</li>
<li>Use GPS equipment (Garmin/Trimble) for field data collection.</li>
<li>Ability to travel to be in the field for extended periods and able to work in rough terrain and challenging weather inclement.</li>
<li>Work independently or as part of a team.</li>
</ul>
VARIOUS DEGREES &amp; SKILLS
<ul>
<li>Master’s or Bachelor’s Degree in Biology or closely related field.</li>
<li>Previous construction monitoring experience in similar California environments.</li>
<li>Knowledge of local, state, and federal environmental regulations.</li>
<li>Team player with the ability to work in a fast-paced environment.</li>
<li>Sound business ethics, including the protection of proprietary and confidential information.</li>
<li>Proficiency in MS Office Applications (Word, PowerPoint, Outlook, Excel) and project tracking software and databases.</li>
<li>Experience with any of the following species: Tipton Kangaroo Rat, San Joaquin Antelope Squirrel, California Tiger Salamander, San Joaquin Kit Fox, Giant Garter Snake</li>
</ul>
We offer a generous benefits package including company-paid medical insurance, paid holidays, 401k and paid time off (PTO)
Upon a conditional job offer, a drug test and background check will be required.
Compensation based on experience.
(Biologists, Biology, GPS, endangered species, field surveys, mammal, amphibian)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

<h3>Job Description</h3>
Job Description
Job Summary:
We are seeking an experienced Chemical process engineer to oversee daily operations at our chemical manufacturing facility. The ideal candidate will have a strong background in chemical engineering, process management, and hands-on experience in formulating, scaling, and producing polymers. This position requires comprehensive knowledge of chemical handling, process safety, and production optimization.
Key Responsibilities:
· Lead, supervise, and coordinate all aspects of plant operations related to polymer synthesis and chemical processing.
· Manage day-to-day plant activities including production scheduling, equipment maintenance, quality control, and personnel oversight.
· Monitor and optimize production processes for efficiency, yield, and quality, particularly in the manufacture of water-based, solvent-based, or specialty polymers.
· Ensure compliance with OSHA, EPA, and other regulatory requirements, including proper chemical handling, storage, and disposal.
· Oversee raw material procurement and inventory control of monomers, catalysts, surfactants, solvents, and other chemicals.
· Work closely with R&amp;D and QA teams to scale up lab-developed polymers to full-scale production.
· Develop and maintain standard operating procedures (SOPs), batch sheets, and safety protocols.
· Train and mentor plant staff in chemical safety, operational procedures, and emergency response.
· Analyze data and implement continuous improvement strategies for process reliability, safety, and cost-effectiveness.
· Manage capital improvement projects, plant expansions, and equipment upgrades.
Qualifications:
· Bachelor’s degree (or higher) in Chemical Engineering, Chemistry, or Polymer Science.
· Minimum 5 years of experience in a chemical or polymer manufacturing plant, with at least 2 years in a supervisory or management role.
· Strong working knowledge of polymerization techniques (e.g., emulsion, suspension, solution, bulk).
· Familiarity with chemical process equipment (reactors, mixers, filtration units, etc.).
· Proficient in chemical handling protocols, hazard communication (GHS), and personal protective equipment (PPE) use.
· Experience with batch processing, process control systems (PLC/SCADA), and ISO/GMP standards is preferred.
· Excellent leadership, communication, and problem-solving skills.
Preferred Skills:
· Experience with waterborne acrylics, polyurethanes, styrene-butadiene, or specialty resin systems.
Work Environment:
· Manufacturing plant environment with regular exposure to chemicals, high temperatures, and production machinery.
· Must be able to wear required PPE and respond to emergencies when necessary.
Compensation &amp; Benefits:
· Competitive salary commensurate with experience
· Health insurance
· SIMPLE IRA (SIRA) retirement plan
· Paid time off and holidays
· Relocation assistance (if applicable)
Job Type: Full-time
Pay: $90,257.70+
Benefits:
<ul>
<li>401(k)</li>
<li>Flexible schedule</li>
<li>Health insurance</li>
<li>Paid time off</li>
</ul>
Schedule:
<ul>
<li>8 hour shift</li>
<li>Monday to Friday</li>
</ul>
Education:
<ul>
<li>Bachelor's (Required)</li>
</ul>

Chemical Process Engineer

<h3>Job Description</h3>
Job Description
About General Fluidics General Fluidics is a clinical diagnostics startup developing the Axess™ platform, a breakthrough point-of-care system that delivers laboratory-grade performance across clinical chemistry, hematology, and immunoassays from a single blood sample. By integrating three “gold standard” analytical technologies into one compact instrument, we are transforming how clinicians access and act on diagnostic data. Learn more at generalfluidics.com.
The Role We are seeking a highly motivated Research Associate to join our R&amp;D team and help expand our menu of diagnostic assays for veterinary and human health applications. This is an R&amp;D-focused laboratory role—ideal for a scientist who thrives on experimental design, assay development, and hands-on instrumentation work. You will design and interpret experiments where answers are unknown, not simply execute QC protocols.
Reporting to the Head of Assay Development, you will work closely with engineers and scientists to optimize assay and instrument performance, generate data for analytical validation, and accelerate our path to regulatory clearance and product launch. This role is best suited for a self-starter who can work independently under mentorship, with the drive to solve problems in a fast-paced, startup environment.
Key Responsibilities
<ul>
<li>
Design, develop, and validate clinical chemistry, hematology, and immunoassays on the Axess™ point-of-care instrument.
</li>
<li>
Independently plan and execute experiments to optimize assay and instrument performance, collaborating closely with engineers on system integration.
</li>
<li>
Perform data analysis and statistical evaluation to guide assay development and regulatory submissions.
</li>
<li>
Author experimental protocols, R&amp;D reports, and supporting documentation.
</li>
<li>
Support quality assurance through calibration, control protocols, and proficiency testing.
</li>
<li>
Work safely with human and animal blood specimens in compliance with biosafety regulations.
</li>
</ul>
Qualifications
<ul>
<li>
Bachelor’s, Master’s, or PhD in biotechnology, biomedical engineering, chemistry, physics, or related field.
</li>
<li>
0–2 years post-PhD or 2–5 years of industry/academic R&amp;D experience (not QC/manufacturing).
</li>
<li>
Experience designing and interpreting experiments, analyzing data, and troubleshooting unexpected results.
</li>
<li>
Hands-on laboratory skills: pipetting, assay development, reagent preparation, use of biosafety cabinets.
</li>
<li>
Familiarity with clinical instrumentation (e.g., flow cytometry, hematology analyzers, clinical chemistry, immunoassays) strongly preferred.
</li>
<li>
Exposure to diagnostic assay development, validation, or instrumentation is a plus.
</li>
<li>
Comfortable in a dynamic startup environment: flexible schedule, ownership mentality, willingness to push projects forward outside a strict 9–5.
</li>
<li>
Excellent communication skills, with the ability to clearly present scientific concepts and data.
</li>
</ul>
Who You Are
<ul>
<li>
Curious, creative, and excited to tackle open-ended scientific questions.
</li>
<li>
Thrives on independence but values mentorship and collaboration.
</li>
<li>
Driven by the opportunity to help build a transformative diagnostic platform from the ground up.
</li>
</ul>
Company DescriptionGeneral Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus. 
<h3>Company Description</h3>
General Fluidics, is a clinical diagnostics company with a novel point-of-care instrument for simultaneous measurement of clinical chemistry, hematology and immunoassays from human and animal blood (<a href="https://www.generalfluidics.com" target="_blank">https://www.generalfluidics.com</a>). We are creating an entirely new category of blood testing technology that brings the quality and menu of the reference laboratory to the point of care. Our AxessTM diagnostic platform seamlessly integrates three “gold standard” analytical technologies to provide full hematology, clinical chemistry and immunoassay test menus.

Research Associate I / II

<h3>Job Description</h3>
Job Description
Chemist I
Precision Analytical (PA), creators of the DUTCH Test, is looking for a Chemist I to help support our company growth and further our mission of providing the best diagnostic tools in functional medicine. PA is an exciting place to develop your skills, take care of client needs, and be a part of a dynamic team.
This position offers career progression within our lab team and entry level candidates are welcomed! Successful candidates will have the ability to learn quickly and effectively, have a passion for quality and an interest in helping others.
This role will work onsite in our McMinnville, OR location.
Please submit a copy of your transcripts along with your resume. This can be an official or unofficial copy. 
Job Summary:
You will be responsible for performing high quality analytical methods in a progressive laboratory. You will provide support for lab analysis through routine sample testing and basic instrument troubleshooting.
Responsibilities:
• Perform analytical methods on patient samples (urine and saliva samples) using UV-vis spectrophotometry, solid phase extractions, hydrolysis and derivatization to prepare samples for instrument analysis
• Prepare standards or reagents needed for analytical procedures
• Regularly observe equipment for any abnormalities, perform basic troubleshooting and maintenance of associated equipment
• Effectively multitask and coordinate multiple assignments simultaneously with a high degree of accuracy and timeliness
• Maintain and follow all laboratory methods, protocols, and SOPs; follow other company procedures, guidelines, and policies
• Communicate effectively and with a sense of urgency quality issues or key findings to the proper supervisor
• Adhere to safety and housekeeping requirements, and communicate concerns to supervisor or manager
• Perform basic office tasks such organizing, filing, copying, emails
• Demonstrate PA’s Core Values in daily activities and interactions with others
• Collaboratively perform other duties as needed to support company goals
Qualifications:
• A Bachelor’s degree with a major in Chemistry, OR equivalent education to include 8 hours of organic chemistry and 4 hours of analytical chemistry, OR analytical chemistry experience through employment
• Computer technology experience and the ability to learn systems quickly and effectively; Precision Analytical uses Microsoft Office (Outlook, Word, Excel, Teams) as well as lab specific systems
• Excellent organizational skills, ability to prioritize multiple responsibilities and strong attention to detail
• Strong interpersonal and listening skills; the ability to communicate (verbal/writing) effectively at all levels and with all customers, internally and externally
• Dependable and punctual; ability to work flexible hours. 90-day training period is Monday through Friday ( 8 hour days, some overtime may be required). After training, this position will be required to work a 4-day, 10-hour schedule Sunday-Wednesday or Wednesday-Saturday determined by company needs.
• Positive teamwork-oriented attitude; champion for our people, culture, company, and brand
Work environment:
This position is located in an office/lab environment with frequent use of laboratory instruments and tools, computer and related hardware. A person must be able to stand and/or sit and effectively move around the building and lab workspaces; see, hear and talk; use hands to type, handle or feel tools or controls; use hands and arms to reach.
This position requires lifting up to 25lbs, and use of PPE when working with urine, saliva, or other samples, or with chemicals and other substances, within our lab environment.
 Four 10-hour shifts either Sunday-Wednesday or Wednesday - Saturday. Training is 10-hour shifts Tuesday - Friday or Monday - Thursday

Chemist I

<h3>Job Description</h3>
Job Descriptionjob summary: 
Radiochemist I or II - permanent FTE role fully onsite in Atlanta, GA. If you are a traditional chemist / nuclear chemist / radiochemist with radiation experience you could fit this role!
You will manufacture radioactive calibration standards, check sources and and check the proficiency of testing samples. Plans and organizes quarterly production of Performance Testing Samples, evaluates data, performs some troubleshooting, and provides support to the traceability program.
 location: Atlanta, Georgia job type: Permanent salary: $68,000 - 70,000 per year work hours: 8 to 4 education: Bachelors responsibilities: 
<ul>
<li>Manufactures calibration standards, check sources and PE samples.</li>
<li>Manufactures sources to support Counting Laboratory and NIST MAP / traceability program.</li>
<li>Produces mixed isotope batches e.g., MGS, TCC, GRS, A/F, and others.</li>
<li>Performs gas and solution calibrations, reviews, and signs Certificates of Calibration.</li>
<li>Maintains laboratory environment, equipment, radionuclide, and chemical inventories.</li>
</ul>
 qualifications: 
-- a 4-year degree in Chemistry with 5 years related experience in radiochemistry and standard preparation.
-- 3 years combining wet radiochemistry (analytical balance operation, dilutions, pipetting),
(basics of nuclear counting methodology and nuclear physics experience a plus)
-- GLP experience
-- Nuclear Data software
#LI-DM1
 skills: Nuclear Magnetic Resonance (NMR) Spectroscopy 
 Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status. At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact <a href="mailto:HRsupport@randstadusa.com" target="_blank">HRsupport@randstadusa.com</a>. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&amp;D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days.

Radiochemist

<h3>Job Description</h3>
Job DescriptionQuality Control ChemistJob Description
We are seeking a dedicated Quality Control Chemist to perform testing and evaluations of raw materials, bulk, and finished products following written procedures. The role involves ensuring compliance with GMP requirements and maintaining accurate documentation records. You will develop an understanding of various testing methodologies and maintain neat and organized work areas.
Responsibilities
<ul>
<li>Perform testing and evaluations of raw materials, bulk, and finished products in accordance with written procedures.</li>
<li>Ensure test results meet current specifications prior to completion and approval.</li>
<li>Troubleshoot out-of-specification situations and perform batch adjustments as needed.</li>
<li>Maintain compliance with current regulatory expectations and practices, such as USP.</li>
<li>Document monthly Key Quality Incidents and out-of-specification situations, determining root causes and suggesting solutions.</li>
<li>Utilize data to focus improvement efforts, ensuring customer requirements and regulatory regulations are met.</li>
<li>Understand and maintain a culture of 'lean action' within the department.</li>
</ul>
Essential Skills
<ul>
<li>4-year degree in Chemistry.</li>
<li>0-2 years of quality control industry experience in pharma, cosmetics, or food.</li>
<li>Proficiency in laboratory techniques such as wet chemistry, FTIR, and quality control.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience with solution preparation, wet chemistry titrations, HPLC, GC, and UV is a plus.</li>
</ul>
 Pay and Benefits
The pay range for this position is $25.00 - $26.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Minneapolis,MN.
Application Deadline
This position is anticipated to close on Sep 1, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Quality Control Chemist

<h3>Job Description</h3>
Job Description
Job Type: Full-Time
Reports To: President and Vice President of Operations
Job Summary:
We are seeking an experienced Chemical Plant Manager to oversee daily operations at our chemical manufacturing facility. The ideal candidate will have a strong background in chemical engineering, process management, and hands-on experience in formulating, scaling, and producing polymers. This position requires comprehensive knowledge of chemical handling, process safety, and production optimization.
Key Responsibilities:
· Lead, supervise, and coordinate all aspects of plant operations related to polymer synthesis and chemical processing.
· Manage day-to-day plant activities including production scheduling, equipment maintenance, quality control, and personnel oversight.
· Monitor and optimize production processes for efficiency, yield, and quality, particularly in the manufacture of water-based, solvent-based, or specialty polymers.
· Ensure compliance with OSHA, EPA, and other regulatory requirements, including proper chemical handling, storage, and disposal.
· Oversee raw material procurement and inventory control of monomers, catalysts, surfactants, solvents, and other chemicals.
· Work closely with R&amp;D and QA teams to scale up lab-developed polymers to full-scale production.
· Develop and maintain standard operating procedures (SOPs), batch sheets, and safety protocols.
· Train and mentor plant staff in chemical safety, operational procedures, and emergency response.
· Analyze data and implement continuous improvement strategies for process reliability, safety, and cost-effectiveness.
· Manage capital improvement projects, plant expansions, and equipment upgrades.
Qualifications:
· Bachelor’s degree (or higher) in Chemical Engineering, Chemistry, or Polymer Science.
· Minimum 5 years of experience in a chemical or polymer manufacturing plant, with at least 2 years in a supervisory or management role.
· Strong working knowledge of polymerization techniques (e.g., emulsion, suspension, solution, bulk).
· Familiarity with chemical process equipment (reactors, mixers, filtration units, etc.).
· Proficient in chemical handling protocols, hazard communication (GHS), and personal protective equipment (PPE) use.
· Experience with batch processing, process control systems (PLC/SCADA), and ISO/GMP standards is preferred.
· Excellent leadership, communication, and problem-solving skills.
Preferred Skills:
· Experience with waterborne acrylics, polyurethanes, styrene-butadiene, or specialty resin systems.
Work Environment:
· Manufacturing plant environment with regular exposure to chemicals, high temperatures, and production machinery.
· Must be able to wear required PPE and respond to emergencies when necessary.
Compensation &amp; Benefits:
· Competitive salary commensurate with experience
· Health insurance
· SIMPLE IRA (SIRA) retirement plan
· Paid time off and holidays
· Relocation assistance (if applicable)
Job Type: Full-time
Pay: $90,257.70+
Benefits:
<ul>
<li>401(k)</li>
<li>Flexible schedule</li>
<li>Health insurance</li>
<li>Paid time off</li>
</ul>
Schedule:
<ul>
<li>8 hour shift</li>
<li>Monday to Friday</li>
</ul>
Application Question(s):
<ul>
<li>Do you have a chemical background?</li>
</ul>
Education:
<ul>
<li>Bachelor's (Required)</li>
</ul>

Chemical Plant Manager

<h3>Job Description</h3>
Job Description
Calgon Carbon | A Kuraray Company is growing—and so can your career. Be part of a global leader in environmental solutions, where your work directly impacts the quality of air and water around the world.
Position: Chemical/Environmental Senior Applications Engineer Location: Remote - Western US
Excellent Benefits:&nbsp;Medical, dental, prescription &amp; vision, HSA &amp; retirement savings (401k) –&nbsp;Generous Company Match! Perks:&nbsp;Incentives/bonus plans, competitive pay, dress for your day, hybrid schedules, paid time off (vacation starting at 3 weeks), tuition reimbursement, wellness programs, fun events, learning &amp; development opportunities.&nbsp;&nbsp;
Hours of work:&nbsp;Full-time position with hours Monday-Friday 9:00-5:00 PM
 The Senior Applications Engineer provides the lead technical support for the sale of carbon, equipment, and service in domestic or international markets. This role interfaces with Equipment Engineering, Research and Development, Equipment and Assembly, Product Management, and Sales to provide the technical justification for the use of activated carbon technology in customer applications. The Senior Applications Engineer will assist in the technical development of emerging markets/applications as it pertains to their area of focus, as well as providing lead technical and business support for key global business development groups. This role can also include supervision of entry or intermediate applications engineers &nbsp; &nbsp;Duties and Responsibilities (not limited to) &nbsp;
<ul>
<li>Uses gained technical expertise, know-how and supplied computer models to select appropriate carbon and equipment for liquid and vapor phase applications, and predict performance based upon customer conditions</li>
<li>Set-up and monitor pilot trials in the field and provide design information for future full-scale systems</li>
<li>Interpret data from the lab and the field trials for pilot and full-scale systems to provide technical design and operational recommendations</li>
<li>Trouble shoot customer problems such as short filter run-times or unexpected breakthrough</li>
<li>Provide application engineering support for a geographic region(s) or set of Technical Sales Reps</li>
<li>Called to work with R&amp;D on the development / testing of new carbon products / applications</li>
<li>May also provide technical guidance to engineers with less experience and to overseas colleagues when called upon</li>
<li>Prepares and provides technical training for TSR when new topics, applications, etc. are encountered</li>
<li>Responsible for other general training and assuring consistency of technical messages from TSRs to customers</li>
<li>In coordination with the Technical Director, Market Development Director, and Sales Director, develop strategies and market-specific approaches to expand existing base business and develop new business opportunities through CCC technology adoption</li>
<li>Regularly review and evaluate actual results, report/troubleshoot variances, adjust strategy as appropriate</li>
<li>Provide technical lead for the Business Unit on CCC global initiatives / cross-business segment groups</li>
<li>Working closely with other CCC global regions on projects covering multiple geographic territories</li>
<li>Acts as technical support and back-up contact related to specific projects for Sales team</li>
<li>Serves as liaison between Sales team and internal support teams including Product and Project Management</li>
<li>Review bid specifications for clarity, accuracy and acceptance</li>
<li>Provide recommendations to improve technical quality of bid specifications and prevent undue risk to Calgon Carbon</li>
<li>Serve as main Calgon Carbon contact to customer when Technical Sales Rep is unable to respond to customer</li>
<li>Participate in Industry forums related to emerging markets and existing applications</li>
<li>Attend technical conferences and trade shows to gain technical knowledge and represent Calgon Carbon as a leader in the activated carbon market</li>
<li>Prepare and present papers/posters at conferences, trade shows and virtual opportunities, e.g. webinars</li>
<li>Develop and present technical presentation / training to engineering consultants, clients, regulators, legislators and others to influence selection of treatment solutions</li>
<li>Attendance at conference would be as lead technical personnel &nbsp;</li>
</ul>
Qualifications
<ul>
<li>A bachelor’s degree (B.A. or B.S.), or equivalent from four-year college or university is required (Chemical Engineering or related engineering/chemistry field)</li>
<li>10+ years&nbsp;of experience in the application of carbon adsorption technology to address customer requirements in liquid and gas purification, including carbon modeling, equipment design and development, and equipment functionality is required</li>
<li>5-7 years&nbsp;of experience in the use and troubleshooting of adsorption equipment at customer sites is required</li>
<li>Experience with business/marketing is preferred.</li>
</ul>
 About Calgon Carbon
At Calgon Carbon, we are scientific innovators with a proud legacy of over 80 years and more than 205 patents to our name. Since pioneering the first activated carbon products from bituminous coal in the 1940s, we’ve been at the forefront of developing cutting-edge technologies and solutions to meet the world’s evolving air and water purification needs.
Today, our portfolio includes more than 700 direct market applications across a wide range of industries. Headquartered in Pittsburgh, Pennsylvania, Calgon Carbon employs approximately 1,685 professionals and operates 20 facilities worldwide dedicated to manufacturing, reactivation, innovation, and equipment fabrication. In Europe, we operate under the name Chemviron.
In March 2018, Calgon Carbon became part of the Kuraray Group. Together, we offer complementary products and services, united by a shared commitment to delivering the highest quality and most innovative activated carbon solutions to customers around the globe.
Calgon Carbon is an Equal Opportunity Employer, including disabled/veteran
 
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